Post Epidural Steroid Injection Follow-up

Status Completed

Clinical Trial Summary

To determine the expected pain response timeline for patients receiving epidural steroid injections, our team plans to assess patient pain severity and degree of pain relief every 3 days for 23 days.

Clinical Trial Description

Patients who are already planning to receive an epidural steroid injection from their physiatrist will be approached by study members on the day of their injection. If enrolled, the patients will be contacted every 3 days for 23 days to determine the severity of pain and degree of pain relief from the injection. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04207606
Study type	Observational
Source	Vanderbilt University Medical Center
Contact
Status	Completed
Phase
Start date	January 3, 2020
Completion date	December 1, 2020

View Details

See also
Status	Clinical Trial	Phase
Recruiting	`NCT04795284` - Biomechanical Parameters of Gait in Patients With Symptomatic Lumbar Spinal Stenosis and Healthy Elderly.
Recruiting	`NCT04066296` - Outcomes for Lumbar Decompressions With Use of Liposomal Bupivicaine	Phase 2
Active, not recruiting	`NCT05114135` - TLIF Osteo3 ZP Putty Study (Also Known as the TOP Fusion Study)	N/A
Recruiting	`NCT06075862` - Balance Amongst Patients With Lumbar Spinal Stenosis
Recruiting	`NCT06057428` - Activity Levels Amongst Patients With Lumbar Spinal Stenosis
Recruiting	`NCT05527145` - Spinal Stenosis and Listhesis Treated With Percutaneous Interspinous Spacer: a Non-surgical Trial	N/A
Recruiting	`NCT01902979` - The Spinal Stenosis Pedometer and Nutrition e-Health Lifestyle Intervention (SSPANLI) Trial	N/A
Completed	`NCT00749073` - The Vertos MILD™ Preliminary Patient Evaluation Study	N/A
Completed	`NCT00527527` - Chiropractic Dosage for Lumbar Stenosis	Phase 2
Completed	`NCT00405691` - Safety and Effectiveness Study of the TOPS System, a Total Posterior Arthroplasty Implant Designed to Alleviate Pain Resulting From Moderate to Severe Lumbar Stenosis	Phase 3
Completed	`NCT03194607` - Quantitative Evaluation of Motor Function Before and After Surgery for Degenerative Lumbar Spinal Stenosis
Recruiting	`NCT06034405` - Analysis of Lumbar Spine Stenosis Specimens for Identification of Transthyretin Cardiac Amyloidosis
Completed	`NCT06079580` - Patients With Lumbar Spinal Stenosis With Balance Disorder
Recruiting	`NCT05523388` - Role of Spinal Load in the Pathophysiology of Lumbar Spinal Stenosis
Completed	`NCT04587401` - The Effects of Anesthesia on Cerebral Perfusion in Patients With High Blood Pressure	N/A
Completed	`NCT04563793` - Postmarket Outcomes Study for Evaluation of the Superion™ Spacer
Suspended	`NCT03381677` - Pedicle Osteotomy for Stenosis Trial	N/A
Completed	`NCT02258672` - Preoperative Rehabilitation for Patients Undergoing Surgery for Lumbar Spinal Stenosis	N/A
Completed	`NCT02260401` - Long Term Outcomes of Lumbar Epidural Steroid Injections for Spinal Stenosis	N/A
Completed	`NCT01994512` - Swedish Spinal Stenosis Study	N/A